FDA Inspection 1192233 — Ace Medical

Ace Medical — FEI 3005126704

The FDA completed an inspection of Ace Medical on Nov 3, 2022 in Goyang. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 3, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Goyang (Korea (the Republic of))

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.